scholarly journals Guillain-Barré Syndrome after Streptokinase Therapy for Acute Myocardial Infarction

2010 ◽  
Vol 49 (22) ◽  
pp. 2445-2446 ◽  
Author(s):  
Ahad Eshraghian ◽  
Hamed Eshraghian ◽  
Kamran Aghasadeghi
2017 ◽  
Vol 33 (2) ◽  
pp. 103-104
Author(s):  
Mohammad Kafil Uddin ◽  
- Md Shahidullah ◽  
Subash Kanti Dey ◽  
Rezaul Karim Khan ◽  
Md Rafiqul Islam ◽  
...  

We would like to report on a patient, a 52-year-old man with acute neurologic disorder, Guillain Barré Syndrome. He was successfully treated by intravenous immunoglobulin. The patient suffered from acute extensive anterior MI. 2 weeks after thrombolytic therapy with streptokinase, he developed GBS. Bangladesh Journal of Neuroscience 2017; Vol. 33 (2): 103-104


2014 ◽  
Vol 11 (2) ◽  
pp. 110-114
Author(s):  
Pankaj Jariwala ◽  
Harikishan Boorugu ◽  
Gopal Chevuru ◽  
Arshad Punjani ◽  
Shaeq Mirza ◽  
...  

2010 ◽  
Vol 2010 ◽  
pp. 1-2
Author(s):  
Ertugrul Okuyan ◽  
Mehmet Akif Cakar ◽  
Mustafa H. Dinckal

Guillain-Barre syndrome (GBS) is an eponym for a heterogeneous group of immune-mediated peripheral neuropathies. We describe a case of GBS in a patient who recieved intravenous streptokinase therapy for acute anterior myocardial infarction. Clinical symptoms are thought to result from streptokinase-antibody complex mediated damage to the local blood-nerve barrier. Patient was treated with 5-days course of intravenous gammaglobulin and his outcome was good.


BMJ ◽  
1987 ◽  
Vol 294 (6572) ◽  
pp. 613-614 ◽  
Author(s):  
A J McDonagh ◽  
J Dawson

2017 ◽  
Vol 4 (3) ◽  
pp. 39
Author(s):  
Joshua Newman ◽  
Andrew Chen ◽  
Saud Rana ◽  
Max Liebo

Guillain-Barré syndrome (GBS) is rare autoimmune polyneuropathy that is infrequently seen in the post-transplant population, presumably due to the presence of immunosuppression. When it does occur in this setting, Cytomegalovirus (CMV) infection is a common inciting factor. Treatment modalities for GBS include intravenous immunoglobulin (IVIg) or plasmapheresis. Rarely, IVIg infusion has been associated with myocardial infarction. We describe a case of a patient status post heart transplantation who presented with GBS shortly after developing CMV viremia. When treatment with IVIg was initiated, our patient developed myocardial infarction with acute cardiac biomarker elevation, acute systolic dysfunction, and cardiogenic shock requiring inotropic and vasopressor support. Coronary angiography demonstrated no significant coronary artery disease. The patient’s cardiac function recovered, as did the GBS following initiation of plasmapheresis. We review prior cases of GBS in transplant patients as well as IVIg associated myocardial infarction.


1990 ◽  
Vol 10 (2) ◽  
pp. 220-221
Author(s):  
K. Ashouri ◽  
A. K. Foli ◽  
A. Singhal

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